Systemic levels of neuropeptide Y and dipeptidyl peptidase activity in patients with Ewing sarcoma—Associations with tumor phenotype and survival
dc.contributor.author | Tilan, Jason U. | en_US |
dc.contributor.author | Krailo, Mark | en_US |
dc.contributor.author | Barkauskas, Donald A. | en_US |
dc.contributor.author | Galli, Susana | en_US |
dc.contributor.author | Mtaweh, Haifa | en_US |
dc.contributor.author | Long, Jessica | en_US |
dc.contributor.author | Wang, Hongkun | en_US |
dc.contributor.author | Hawkins, Kirsten | en_US |
dc.contributor.author | Lu, Congyi | en_US |
dc.contributor.author | Jeha, Dima | en_US |
dc.contributor.author | Izycka‐swieszewska, Ewa | en_US |
dc.contributor.author | Lawlor, Elizabeth R. | en_US |
dc.contributor.author | Toretsky, Jeffrey A. | en_US |
dc.contributor.author | Kitlinska, Joanna B. | en_US |
dc.date.accessioned | 2015-03-05T18:24:33Z | |
dc.date.available | 2016-05-10T20:26:27Z | en |
dc.date.issued | 2015-03-01 | en_US |
dc.identifier.citation | Tilan, Jason U.; Krailo, Mark; Barkauskas, Donald A.; Galli, Susana; Mtaweh, Haifa; Long, Jessica; Wang, Hongkun; Hawkins, Kirsten; Lu, Congyi; Jeha, Dima; Izycka‐swieszewska, Ewa ; Lawlor, Elizabeth R.; Toretsky, Jeffrey A.; Kitlinska, Joanna B. (2015). "Systemic levels of neuropeptide Y and dipeptidyl peptidase activity in patients with Ewing sarcomaâ Associations with tumor phenotype and survival." Cancer 121(5): 697-707. | en_US |
dc.identifier.issn | 0008-543X | en_US |
dc.identifier.issn | 1097-0142 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/110734 | |
dc.publisher | Wiley Periodicals, Inc. | en_US |
dc.subject.other | survival | en_US |
dc.subject.other | Ewing sarcoma | en_US |
dc.subject.other | neuropeptide Y | en_US |
dc.subject.other | dipeptidyl peptidase IV | en_US |
dc.subject.other | disease phenotype | en_US |
dc.title | Systemic levels of neuropeptide Y and dipeptidyl peptidase activity in patients with Ewing sarcoma—Associations with tumor phenotype and survival | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Oncology and Hematology | en_US |
dc.subject.hlbsecondlevel | Public Health | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/110734/1/cncr29090.pdf | |
dc.identifier.doi | 10.1002/cncr.29090 | en_US |
dc.identifier.source | Cancer | en_US |
dc.identifier.citedreference | Dotsch J, Christiansen H, Hanze J, Lampert F, Rascher W. Plasma neuropeptide Y of children with neuroblastoma in relation to stage, age and prognosis, and tissue neuropeptide Y. Regul Pept. 1998; 75‐76: 185 – 190. | en_US |
dc.identifier.citedreference | Ladenstein R, Potschger U, Le Deley MC, et al. Primary disseminated multifocal Ewing sarcoma: results of the Euro‐EWING 99 trial. J Clin Oncol. 2010; 28: 3284 – 3291. | en_US |
dc.identifier.citedreference | Womer RB, West DC, Krailo MD, et al. Randomized controlled trial of interval‐compressed chemotherapy for the treatment of localized Ewing sarcoma: a report from the Children's Oncology Group. J Clin Oncol. 2012; 30: 4148 – 4154. | en_US |
dc.identifier.citedreference | Bernstein M, Kovar H, Paulussen M, et al. Ewing's sarcoma family of tumors: current management. Oncologist. 2006; 11: 503 – 519. | en_US |
dc.identifier.citedreference | van Doorninck JA, Ji L, Schaub B, et al. Current treatment protocols have eliminated the prognostic advantage of type 1 fusions in Ewing sarcoma: a report from the Children's Oncology Group. J Clin Oncol. 2010; 28: 1989 – 1994. | en_US |
dc.identifier.citedreference | Antonescu C. Round cell sarcomas beyond Ewing: emerging entities. Histopathology. 2014; 64: 26 – 37. | en_US |
dc.identifier.citedreference | Hancock JD, Lessnick SL. A transcriptional profiling meta‐analysis reveals a core EWS‐FLI gene expression signature. Cell Cycle. 2008; 7: 250 – 256. | en_US |
dc.identifier.citedreference | Lee EW, Michalkiewicz M, Kitlinska J, et al. Neuropeptide Y induces ischemic angiogenesis and restores function of ischemic skeletal muscles. J Clin Invest. 2003; 111: 1853 – 1162. | en_US |
dc.identifier.citedreference | Lu C, Everhart L, Tilan J, et al. Neuropeptide Y and its Y2 receptor: potential targets in neuroblastoma therapy. Oncogene. 2010; 29: 5630 – 5642. | en_US |
dc.identifier.citedreference | Son MY, Kim MJ, Yu K, Koo DB, Cho YS. Involvement of neuropeptide Y and its Y1 and Y5 receptors in maintaining self‐renewal and proliferation of human embryonic stem cells. J Cell Mol Med. 2011; 15: 152 – 165. | en_US |
dc.identifier.citedreference | Lee NJ, Herzog H. NPY regulation of bone remodelling. Neuropeptides. 2009; 43: 457 – 463. | en_US |
dc.identifier.citedreference | Kitlinska J, Abe K, Kuo L, et al. Differential effects of neuropeptide Y on the growth and vascularization of neural crest‐derived tumors. Cancer Res. 2005; 65: 1719 – 1728. | en_US |
dc.identifier.citedreference | Lu C, Tilan JU, Everhart L, et al. Dipeptidyl peptidases as survival factors in Ewing sarcoma family of tumors: implications for tumor biology and therapy. J Biol Chem. 2011; 286: 27494 – 27505. | en_US |
dc.identifier.citedreference | Tilan JU, Lu C, Galli S, et al. Hypoxia shifts activity of neuropeptide Y in Ewing sarcoma from growth‐inhibitory to growth‐promoting effects. Oncotarget. 2013; 4: 2487 – 2501. | en_US |
dc.identifier.citedreference | Cohen PS, Cooper MJ, Helman LJ, Thiele CJ, Seeger RC, Israel MA. Neuropeptide Y expression in the developing adrenal gland and in childhood neuroblastoma tumors. Cancer Res. 1990; 50: 6055 – 6061. | en_US |
dc.identifier.citedreference | Kogner P, Bjork O, Theodorsson E. Plasma neuropeptide Y in healthy children: influence of age, anaesthesia and the establishment of an age‐adjusted reference interval. Acta Paediatr. 1994; 83: 423 – 427. | en_US |
dc.identifier.citedreference | deS Senanayake P, Denker J, Bravo EL, Graham RM. Production, characterization, and expression of neuropeptide Y by human pheochromocytoma. J Clin Invest. 1995; 96: 2503 – 2509. | en_US |
dc.identifier.citedreference | Mentlein R. Dipeptidyl‐peptidase IV (CD26)—role in the inactivation of regulatory peptides. Regul Pept. 1999; 85: 9 – 24. | en_US |
dc.identifier.citedreference | Stulc T, Sedo A. Inhibition of multifunctional dipeptidyl peptidase‐IV: is there a risk of oncological and immunological adverse effects? Diabetes Res Clin Pract. 2010; 88: 125 – 131. | en_US |
dc.identifier.citedreference | Wirth MJ, Patz S, Wahle P. Transcellular induction of neuropeptide Y expression by NT4 and BDNF. Proc Natl Acad Sci U S A. 2005; 102: 3064 – 3069. | en_US |
dc.identifier.citedreference | Yamashiro T, Fukunaga T, Yamashita K, Kobashi N, Takano‐Yamamoto T. Gene and protein expression of brain‐derived neurotrophic factor and TrkB in bone and cartilage. Bone. 2001; 28: 404 – 409. | en_US |
dc.identifier.citedreference | Granchi D, Baglio SR, Amato I, Giunti A, Baldini N. Paracrine inhibition of osteoblast differentiation induced by neuroblastoma cells. Int J Cancer. 2008; 123: 1526 – 1535. | en_US |
dc.identifier.citedreference | Grouzmann E, Fathi M, Gillet M, et al. Disappearance rate of catecholamines, total metanephrines, and neuropeptide Y from the plasma of patients after resection of pheochromocytoma. Clin Chem. 2001; 47: 1075 – 1082. | en_US |
dc.identifier.citedreference | Kogner P, Bjork O, Theodorsson E. Neuropeptide Y in neuroblastoma: increased concentration in metastasis, release during surgery, and characterization of plasma and tumor extracts. Med Pediatr Oncol. 1993; 21: 317 – 322. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
Files in this item
Remediation of Harmful Language
The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.
Accessibility
If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.